rs139407567

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs139407567(C;T)

Make rs139407567(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67490807

Gene	AIP, MIR6752

is a	snp
is	mentioned by
dbSNP	rs139407567
dbSNP (classic)	rs139407567
ClinGen	rs139407567
ebi	rs139407567
HLI	rs139407567
Exac	rs139407567
Gnomad	rs139407567
Varsome	rs139407567
LitVar	rs139407567
Map	rs139407567
PheGenI	rs139407567
Biobank	rs139407567
1000 genomes	rs139407567
hgdp	rs139407567
ensembl	rs139407567
geneview	rs139407567
scholar	rs139407567
google	rs139407567
pharmgkb	rs139407567
gwascentral	rs139407567
openSNP	rs139407567
23andMe	rs139407567
SNPshot	rs139407567
SNPdbe	rs139407567
MSV3d	rs139407567
GWAS Ctlg	rs139407567

Max Magnitude

0

ClinVar
Risk	rs139407567(T;T)
Alt	rs139407567(T;T)
Reference	Rs139407567(C;C)
Significance	Pathogenic
Disease	Somatotroph adenoma Familial Isolated Pituitary Adenomas
Variation	info
Gene	MIR6752 AIP
CLNDBN	Somatotroph adenoma Familial Isolated Pituitary Adenomas
Reversed	0
HGVS	NC_000011.9:g.67258278C>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034108.2, RCV000338604.1,